Two experiments were conducted to examine the effect of growth rate to similar age or BW on fat deposition in stocker cattle grazing dormant native range (DNR) or winter wheat pasture (WP). In each experiment, fall-weaned Angus steers were randomly allotted to 1 of 4 stocker production programs: 1) control, 1.02 kg/d of a 40% CP cottonseed meal-based supplement during grazing of DNR (CON); 2) corn/soybean meal-based supplement fed at 1% of BW during grazing of DNR (CORN); 3) grazing WP at a high stocking rate to achieve a low rate of BW gain (LGWP); and 4) grazing WP at a low stocking rate to achieve a high rate of BW gain (HGWP). In Exp. 1, a subset of steers (3 steers per treatment) was harvested after winter grazing (138 d) at similar age. The remaining WP steers were transitioned into the finishing phase, whereas DNR steers were allowed to graze the same native range pastures for another 115 d without supplementation before entering the feedyard. In Exp. 2, steers grazed their respective pastures until each treatment reached an estimated HCW of 200 kg (262, 180, 142, and 74 d, respectively, for the CON, CORN, LGWP, and HGWP treatments), at which time a subset of steers (4 steers per treatment) were selected for intermediate harvest before finishing. In both experiments, the remaining steers were fed a finishing diet to a common 12th-rib fat thickness of 1.27 cm. In Exp. 1, winter grazing ADG was 0.19, 0.52, 0.68, and 1.37 ± 0.03 kg/d; and in Exp. 2, winter/summer grazing ADG was 0.46, 0.61, 0.83, and 1.29 ± 0.02 kg/d, respectively for CON, CORN, LGWP, and HGWP treatments. At intermediate harvest in Exp. 1, HGWP steers had greater (P < 0.01) 12th-rib fat thickness and marbling scores, compared with the other treatments. However, in Exp. 2, LGWP steers had greater (P < 0.01) marbling scores compared with HGWP steers, which were greater than DNR steers. At final harvest in Exp. 1, LGWP steers had greater (P < 0.01) 12th-rib fat thickness and smaller LM area, compared with the other treatments; however, there were no differences (P = 0.99) in final marbling scores. In Exp. 2, CON steers had lower (P < 0.05) 12th-rib fat thickness and tended (P = 0.10) to have greater marbling scores, compared with the other treatments. These data suggest that changes in the partitioning of fat among depots during the stocker phase may not be reflected after finishing when steers are fed to a common 12th-rib fat thickness.

Sixteen ruminally cannulated crossbred steers (529 ± 45 kg initial body weight, BW) were used to evaluate in situ dry matter (DM), neutral detergent fiber (aNDF), and N degradation characteristics of low-quality prairie hay, blood urea-N (BUN) and rumen fermentation parameters in steers provided a protein supplement with or without Micro-Aid ® (MA; plant derived saponin). Steers were allowed ad libitum access to chopped prairie hay (49 g crude protein (CP)/kg DM and 738 g aNDF/kg DM) and randomly assigned to one of four treatments: (1) no supplement (C), (2) cottonseed meal and wheat middlings: 920 g DM/d (PC; positive control), (3) MA added to PC to supply 1 g MA/d (MA1), and (4) MA added to PC to supply 2 g MA/d (MA2). Steers were individually supplemented 920 g DM once daily at 08:00 along with a vitamin and mineral mix to ensure requirements were met. Orthogonal contrasts were used to determine the effects of protein supplementation, addition of MA and level of MA inclusion. During in situ phase, forage samples were incubated for a 96 h period. Protein supplementation increased DM intake (DMI), particulate passage rate (Kp), and rumen digestibility of DM and NDF (P < 0.001), but there was no effect on rumen N degradability. The inclusion of MA did not impact DMI in either phase. Compared to PC, MA decreased K p (27.8 and 22.7 g DM/kg/h, respectively; P = 0.02), resulting in an increase in rumen aNDF and DM digestibility (P < 0.001). However, there was no influence of MA on apparent total tract digestibility in the metabolism phase. Rumen protozoa concentrations were suppressed (P = 0.01) with MA inclusion while lactate concentrations and microbial crude protein (MCP) flow to the small intestine were increased (P = 0.05). There was no impact on BUN, rumen ammonia, pH, volatile fatty acid (VFA) concentrations or N balance for MA compared to PC diets. Supplementation improved N balance, MCP synthesis and increased total concentrations of VFA and independent acetate and propionate concentrations. In conclusion, including MA in protein supplements increased rumen DM and a NDF digestibility of forage, reduced protozoa concentrations and increased daily outflow of MCP. This is indicative of increased rumen fermentation rate and may ultimately impact animal performance via increased energy and amino acid supply to the small intestine. However, more research is needed to validate this potential impact on animal performance.

Feeding yeast culture fermentation products has been associated with improved feed intake and milk yield in transition dairy cows. These improvements in performance have been further described in terms of rumen characteristics, metabolic profile, and immune response. The objective of this study was to evaluate the effects of a commercial yeast culture product (YC; Culture Classic HD, Phibro Animal Health) on performance, blood biomarkers, rumen fermentation, and rumen bacterial population in dairy cows from −30 to 50 d in milk (DIM). Forty Holstein dairy cows were enrolled in a randomized complete block design from −30 to 50 DIM and blocked according to expected calving day, parity, previous milk yield, and genetic merit. At −30 DIM, cows were assigned to either a basal diet plus 114 g/d of ground corn (control; n = 20) or a basal diet plus 100 g/d of ground corn and 14 g/d of YC (n = 20), fed as a top-dress. Cows received the same close-up diet from 30 d prepartum until calving [1.39 Mcal/kg of dry matter (DM) and 12.3% crude protein (CP)] and lactation diet from calving to 50 DIM (1.60 Mcal/kg of DM and 15.6% CP). Blood samples and rumen fluid were collected at various time points from −30 to 50 d relative to calving.Cows fed YC compared with control showed a trend for increased energy-corrected milk (+3.2 kg/d). Lower somatic cell counts were observed in YC cows than in control. We detected a treatment × time interaction in nonesterified fatty acids (NEFA) that could be attributed to a trend for greater NEFA in YC cows than control at 7 DIM, followed by lower NEFA in YC cows than control at 14 and 30 DIM. In the rumen, YC contributed to mild changes in rumen fermentation, mainly increasing postpartal valerate while decreasing prepartal isovalerate. This was accompanied by alterations in rumen microbiota, including a greater abundance of cellulolytic (Fibrobacter succinogenes) and lactate-utilizing bacteria (Megasphaera elsdenii). These results describe the potential benefits of supplementing yeast culture during the late pregnancy through early lactation, at least in terms of rumen environment and performance.

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